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Home » BLOGS » Cheerful Oncologist

THE CHEERFUL ONCOLOGIST 

“I Can’t Afford Any More Advances in Cancer Care, Doc!”

By Craig R. Hildreth, MD | January 28, 2013
Dr. Hildreth is a medical oncologist in private practice.

One of my patients stopped by this afternoon and, not seeing him on my schedule, I asked my nurse what was the occasion.

“He’s picking up his abiraterone prescription,” she said. Then, with the slightest hesitation she added, “His copay is One of my patients stopped by this afternoon and, not seeing him on my schedule, I asked my nurse what was the occasion.

,300 this month, and it will go up even more after that.”

Dr. Hildreth is a medical oncologist in private practice
(MORE: “This Is My Last Day on Earth”)

The look on my face, according to witnesses, was identical to one who just realized that he had left his wallet in an airport restroom—$2,300 per month for a pill? Granted, this new treatment for metastatic castration-resistant prostate cancer is a major advance, as well as a paradigm for exploiting the tumor’s addiction to androgens; in my patient’s case, abiraterone will double his progression-free survival compared to placebo. The cost, however, takes one’s breath away. Why is this oral medicine, as well as many other exciting new drugs, so expensive to patients?

Those who follow health care insurance updates know the answer—while intravenous chemotherapy is covered as a medical benefit by payors, which therefore limits patient copays and caps the annual overall expense at a certain amount, oral anticancer medicines are reimbursed as a pharmacy benefit. The reality is that new biological agents are often priced like a Ferrari, and patients who are covered under a pharmacy benefit are required to fork over not a fixed copay but a percentage of the pill’s cost, each and every month ‘til eternity or death, whichever comes first. Doing the math at 25%, we conclude that my patient is on a drug that costs $9,200 per month. Yikes!

Doesn’t seem fair, does it? You are not the only one to conclude this. Eighteen states and the District of Columbia have passed laws forcing health insurance companies to cover oral anticancer medications “under terms no less favorable” than those that are administered intravenously. This concept is called oral parity. It is designed to rectify the obvious conclusion that the more money cancer patients have to pay out of their own pocket, the less likely they are to receive their treatment. The converse of this conclusion is called “ensuring access to cancer care,” and I dare you to show me one person in America who doesn’t support such a noble cause.

Ahem—actually I can show you several persons, and they just happen to run health insurance companies. Their response to oral parity has been, to be generous, inconsistent. Payors claim that oral parity laws are a forced mandate to provide benefits, but they are in favor of the Obamacare mandate that all individuals purchase their health insurance. Payors claim that oral parity laws will drive up insurance premiums, but premiums are already rising since the passage of the Affordable Care Act, and according to a detailed report by the Milliman consulting group, parity will raise the average cost of a commercial plan at most by only 0.16% ($0.50 increase per member per month [PMPM] in a $300 PMPM plan).

The advances in oral biological agents that can arrest the growth of obdurate cancers like malignant melanoma are nothing short of well, let’s just say promising. Let’s even say extremely promising. Research uncovers more and more targets on cancer cells that dare us to try and disable them, and we are happy to take up that dare. With the unraveling of the human genome, medical oncology has an opportunity to fulfill the definition of evolution: “a process of continuous change from a lower, simpler, or worse, to a higher, more complex, or better state.” In the fight against cancer, oral targeted agents represent the great leap forward. In order to make this a reality, not to mention continue the complex process of improving efficacy, these medications must reach their intended patients with a minimum of obstruction. Without oral parity, the new horizon in cancer treatment is at risk for stagnation, and if stagnation slows its evolution, medical oncology may eventually limp toward extinction.

 

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by Kim Spencer | February 11, 2013 12:18 PM EST

As a helath care provider and a cancer patient I found this to be a great article. I just wanted to point out another area that impacted my care. That was the cost of injectable drugs. I had reached my max out of pocket with my insurance company. I always thought that when you reached max out of pocket everything would be covered at 100%, I quickly learned that was not the case. I was still responsible for my co-pays for office visits and the 20% of my neulasta. When I called my insurance company I was told that injectable are never covered at 100%. So, my portion after they paid their 80% was $745 per injection (I received four).

by Ahmed Elzawawy | February 08, 2013 1:52 PM EST

I invite you to read about the Win-Win scientific initiative that aims at increasing the affordability of better value cancer treatment . It is available at : http://www.icedoc.org/winwin.htm
Looking to having your feedback. Sincerely, Ahmed Elzawawy, MD. www.icedoc.org

by Carol Cowan | February 08, 2013 1:02 PM EST

In England, the National Health Service, their publicly funded health insurance system, disallows sorafenib (oral) and bevacuzimab (IV) for routine use in treating cancer. A clinical trial using sorafenib used to treat HCC was halted to give the control group access to the drug after it was discovered that overall survival was increased by almost 5 months. The cost of each of those drugs is about $100,000./yr. Here in the US, some doctors don't even prescribe the drugs because they know the cost will be denied by health insurance and their patients can't afford them. While we wait for policy changes to make oral cancer drugs affordable through lower copays and wider acceptance by health insurance companies, there are patient assistance methods that may help. The makers of the drugs may significantly reduce the cost if a strong case is made. My brother-in-law, an HCC patient with an income of $100,000./yr was given courses of bevacuzamab for free by the manufacturer, not once, but twice.

by John Leung | February 08, 2013 10:56 AM EST

There are much cheaper drugs round the corner.
Metformin improves the overall survival of ovarian cancer (and several other cancers) by up to 6x.
Statins double or triple (depending on whether you use a lipophilic or hydrophilic version) the OR of inflammatory breast cancer.
Aspirin, valproic acid, and many other established drugs have the possible side effect of cancer suppression.
For the same reason, the notoriious Thalidomide should be given a second chance.
All these drugs cost a tiny fraction of the "new drugs"that lucrative pharmaceutical firms want to hard sell, and probably try to discourage their "off label" development.
May be it is time for doctors and patients to stand up and fight for cheaper and equally effective, if not more effective anti-cancer drugs.
This will save many more lives, as well as the economy of the society.

by steven kussin | February 08, 2013 10:26 AM EST

Doc, I hope your blog was good. It sounded great. But this site held me captive with a pop up ad that promised to free me by closing it or waiting 20 seconds all options obnoxious and neither strategy worked. This site is a mobile device disaster and a shilling screaming site for ads. Sorry I couldn't read it. I registered just to tell you and then unregistered from this unworthy site

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CHEERFUL ONCOLOGIST

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